Search

We print a tunable photopolymer (photopolymer dispersed liquid crystal -PDLC), using the laser-induced direct transfer technique without absorber layer, which was a challenge for this technique given the low absorption and high viscosity of PDLC, and which had not been achieved so far to our knowledge. This makes the LIFT printing process faster and cleaner and achieves a high-quality printed droplet (aspheric profile and low roughness). A femtosecond laser was needed to reach sufficiently peak energies to induce nonlinear absorption and eject the polymer onto a substrate. Only a narrow energy window allows the material to be ejected without spattering.

Precise characterization of parallel-aligned liquid crystal on silicon microdisplays has an important impact in many advanced photonics applications. We show liquid crystal on silicon (LCoS) modeled as a non-absorbent reciprocal device. Combined with time-average Stokes polarimetry, LCoS enables us to demonstrate robust measurements across the whole applied voltage range for the retardance and its flicker, and also as a novelty for the director orientation. We obtain that the director orientation changes across the voltage range, especially at larger applied voltages. This is a small effect, but it may provide a deeper insight into the internal dynamics in the liquid crystal layer, and in sensitive phase-only applications will produce a coupling between amplitude and phase.

We demonstrate a complete semiphysical and analytical model describing the angular and wavelength dependencies not only of retardance, but also its flicker, in parallel aligned liquid crystal (PA-LC) devices. It relies on the fitting of the molecules' equivalent tilt angle as a function of applied voltage. The wide range of calculations it offers without requiring extensive characterization makes the model unique. We focus on PA-LCoS application as a polarization state generator across the visible spectrum and for a wide range of incidence angles. This approach offers novel capabilities for managing arbitrary states of both full and partial polarization. To highlight the richness of situations with PA-LCoS devices, we provide results for two different digital addressing sequences producing different levels of flicker.

The possibilities that offer the holographic optical elements for photovoltaic and "see through display" applications open new windows for holographic recording materials. In this sense, some specific characteristics are required for each particular application. Waveguides are one of the key elements for these applications. Photopolymers are one of the most competitive candidates for waveguide fabrication. In this work, we evaluate the performance of one example from each of three families of photopolymer material in fabrication of a 633nm waveguide. Firstly, polyvinyl alcohol acrylamide, PVA/AA, the second one, a nanoparticle-thiol-ene, NPC, and on the last place a penta/hexa-acrylate based polymer with dispersed nematic liquid crystal molecules, PDLC. We study the critical role of the material and in particular, spatial resolution for this application.

In recent works, we demonstrated the accuracy and physical relevance of a highly simplified reverse-engineering analytical model for a parallel-aligned liquid crystal on silicon devices (PA-LCoS). Both experimental measurements and computational simulations applying the rigorous split-field finite difference time domain (SF-FDTD) technique led to this conclusion in the low applied voltages range. In this paper, we develop a complete rigorous validation covering the full range of possible applied voltages, including highly non-linear liquid crystal (LC) tilt angle profiles. We demonstrate the applicability of the model for spectral and angular retardation calculations, of interest in spatial light modulation applications. We also show that our analytical model enables the calculation of the retardance for novel PA-LC devices as a function of the LC compound and cell gap, becoming an appealing alternative to the usual numerical approaches for PA-LC devices design.

Photopolymers can be appealing materials for diffractive optical elements fabrication. In this paper, we present the recording of diffractive lenses in PVA/AA (Polyvinyl alcohol acrylamide) based photopolymers using a liquid crystal device as a master. In addition, we study the viability of using a diffusion model to simulate the lens formation in the material and to study the influence of the different parameters that govern the diffractive formation in photopolymers. Once we control the influence of each parameter, we can fit an optimum recording schedule to record each different diffractive optical element with the optimum focalization power.

We focus on the novelty of three elements in holographic data storage systems (HDSS): the data pager, where we introduce a parallel-aligned liquid crystal on silicon (PA-LCoS) microdisplay; the recording material, where we consider the highly versatile PVA/AA photopolymer; and also in the architecture of the object arm, where a convergent correlator system is introduced. We show that PA-LCoS devices cannot implement pure hybrid-ternary modulated (HTM) data pages but a rather close approximation. Validation of the HDSS expressions for the convergent correlator and comparison with the widespread 4-f system is performed. Experimental results with PVA/AA material showing bit-error rates (BER) in the range of 10 -3 , further show its potential application for HDSS, and also demonstrate the validity of the testing platform and PA-LCoS calibration and optimization.

Parallel-aligned (PA) liquid-crystal on silicon (LCoS) microdisplays are especially appealing in a wide range of spatial light modulation applications since they enable phase-only operation. Recently we proposed a novel polarimetric method, based on Stokes polarimetry, enabling the characterization of their linear retardance and the magnitude of their associated phase fluctuations or flicker, exhibited by many LCoS devices. In this work we apply the calibrated values obtained with this technique to show their capability to predict the performance of spatially varying phase multilevel elements displayed onto the PA-LCoS device. Specifically we address a series of multilevel phase blazed gratings. We analyze both their average diffraction efficiency ("static" analysis) and its associated time fluctuation ("dynamic" analysis). Two different electrical configuration files with different degrees of flicker are applied in order to evaluate the actual influence of flicker on the expected performance of the diffractive optical elements addressed. We obtain a good agreement between simulation and experiment, thus demonstrating the predictive capability of the calibration provided by the average Stokes polarimetric technique. Additionally, it is obtained that for electrical configurations with less than 30° amplitude for the flicker retardance, they may not influence the performance of the blazed gratings. In general, we demonstrate that the influence of flicker greatly diminishes when the number of quantization levels in the optical element increases.

Recently we proposed a novel polarimetric method, based on Stokes polarimetry, enabling the characterization of the linear retardance and its flicker amplitude in electro-optic devices behaving as variable linear retarders. In this work we apply extensively the technique to parallel-aligned liquid crystal on silicon devices (PA-LCoS) under the most typical working conditions. As a previous step we provide some experimental analysis to delimitate the robustness of the technique dealing with its repeatability and its reproducibility. Then we analyze the dependencies of retardance and flicker for different digital sequence formats and for a wide variety of working geometries.

A polarimetric method for the measurement of linear retardance in the presence of phase fluctuations is presented. This can be applied to electro-optic devices behaving as variable linear retarders. The method is based on an extended Mueller matrix model for the linear retarder containing the time-averaged effects of the instabilities. As a result, an averaged Stokes polarimetry technique is proposed to characterize both the retardance and its flicker magnitude. Predictive capability of the approach is experimentally demonstrated, validating the model and the calibration technique. The approach is applied to liquid crystal on silicon displays (LCoS) using a commercial Stokes polarimeter. Both the magnitude of the average retardance and the amplitude of its fluctuation are obtained for each gray level value addressed, thus enabling a complete phase characterization of the LCoS.

Photopolymer are appealing materials for diffractive elements recording. Two of their properties when they are illuminated are useful for this goal: the relief surface changes and the refractive index modifications. To this goal the linearity in the material response is crucial to design the optimum irradiance for each element. In this paper we measured directly some parameters to know how linear is the material response, in terms of the refractive index modulation versus exposure, then we can predict the refractive index distributions during recording. We have analyzed at different recording intensities the evolution of monomer diffusion during recording for photopolymers based on PVA/Acrylamide. This model has been successfully applied to PVA/Acrylamide photopolymers to predict the transmitted diffracted orders and the agreement with experimental values has been increased.

Relief surface changes provide interesting possibilities for storing diffractive optical elements on photopolymers and are an important source of information for characterizing and understanding the material behavior. In this paper we use a 3-dimensional model, based on direct parameter measurements, for predicting the relief structures generated on without-coverplate photopolymers. We have analyzed different spatial frequency and recording intensity distributions such as binary and blazed periodic patterns. This model was successfully applied to different photopolymers with different values of monomer diffusion.

Relief surface changes provide interesting possibilities for storing diffractive optical elements on photopolymers and are an important source of information to characterize and understand the material behaviour. In this paper we present a 3-dimensional model based on direct measurements of parameters to predict the relief structures generated on the material. This model is successfully applied to different photopolymers with different values of monomer diffusion. The importance of monomer diffusion in depth is also discussed.

Molecular diffusion effects have been widely studied inside photopolymers for holographic applications. Recently some works have focused on low spatial frequencies to evaluate in real time the monomer diffusion effects. Assuming a Fermi-Dirac function-based profile, we have fitted the diffracted intensities, reflected and transmitted (up to the 8th order), to obtain the phase and surface profile of the recorded gratings. We have studied the influence of diffusion in polyvinyl-alcohol/acrylamide for the range of spatial frequencies between 2 lines/mm and 6 lines/mm. We have demonstrated the influence of the spatial frequency on the magnitude and sign of the material volume variations. We also studied in dark the evolution of the grating shape. We show that it is possible to achieve diffractive gratings with diffraction efficiency in the first order near 35% if the in dark evolution is taken into account. Furthermore we present a method to calculate the monomer diffusivity in photopolymers. The differential equation is deduced and solved, and experimental average value is obtained (D=1.1 x 10(-8) cm(2)s(-1)).

Photopolymers are appealing materials for the fabrication of diffractive optical elements (DOEs). We evaluate the possibilities of polyvinyl-alcohol/acrylamide-based photopolymers to store diffractive elements with low spatial frequencies. We record gratings with different spatial frequencies in the material and analyze the material behavior measuring the transmitted and the reflected orders as a function of exposition. We study two different compositions for the photopolymer, with and without a cross-linker. The values of diffraction efficiency achieved for both compositions make the material suitable to record DOEs with long spatial periods. Assuming a Fermi-Dirac-function-based profile, we fitted the diffracted intensities (up to the eighth order) to obtain the phase profile of the recorded gratings. This analysis shows that it is possible to achieve a phase shift larger than 2pi rad with steep edges in the periodic phase profile. In the case of the measurements in reflection, we have obtained information dealing with the surface profile, which show that it has a smooth shape with an extremely large phase-modulation depth.

In a holographic recording is advisable that the diffraction efficiency increases linearly with the exposure in a wide zone of the curve of diffraction efficiency versus energetic exposure and the slope of the curve must be approximately constant before saturation in order to improve the energetic sensitivity and to get reproducibility in different recordings with the same kind of photopolymer, although to find examples of deviations to this behavior it is usual. The more important deviation experimentally observed in photopolymers with high thickness happen when the first maximum in the curve is lower than the second one. This effect is opposed to an overmodulation. We present a main hypothesis related to the dye concentration into the layer and with the molecular weight of the polymer chains generated in the polymerization process in order to explain this effect.

Holographic data pages were multiplexed in different thickness layers of a polyvinyl alcohol/acrylamide photopolymer. This material is formed of acrylamide photopolymers, which are considered interesting materials for recording holographic memories. A liquid crystal device was used to modify the object beam and store the data pages. A peristrophic multiplexing method is used to store a large number of data pages in the same spot in the material. The bit error rate was calculated fitting the histograms of the images to determine what parameters improve the quality of the images.

One of the problems associated with photopolymers as optical recording media is the thickness variation during the recording process. Different values of shrinkages or swelling are reported in the literature for photopolymers. Furthermore, these variations depend on the spatial frequencies of the gratings stored in the materials. Thickness variations can be measured using different methods: studying the deviation from the Bragg's angle for nonslanted gratings, using MicroXAM S/N 8038 interferometer, or by the thermomechanical analysis experiments. In a previous paper, we began the characterization of the properties of a polyvinyl alcohol/acrylamide based photopolymer at the lowest end of recorded spatial frequencies. In this work, we continue analyzing the thickness variations of these materials using a reflection interferometer. With this technique we are able to obtain the variations of the layers refractive index and, therefore, a direct estimation of the polymer refractive index.

We characterize the optical modulation properties of a polyvinyl alcohol/acrylamide (PVA/AA) photopolymer at the lowest end of recorded spatial frequencies. To achieve this goal we have constructed a double beam interferometer in combination with the setup to expose the recording material. This is a novel approach since usually holographic recording materials are only characterized at high spatial frequencies. Some benefits are provided by the approach we propose: a direct calculation of the properties of the material is possible, and on the other hand additional information can be obtained since the results are not influenced by diffusion processes. Furthermore, this characterization is needed to optimize the PVA/AA photopolymers for another range of applications, such as recording of diffractive optical elements, where very low spatial frequencies are recorded. Different PVA/AA compositions and layer thicknesses have been analyzed. We have found that, depending on the layer characteristics, we can achieve high values of the phase-shift modulation depth and enhance the sensitivity of the material.

We show an accurate procedure to obtain a Fourier transform (FT) with no dc term using a commercial twisted-nematic liquid-crystal display. We focus on the application to holographic storage of binary data pages, where a drastic decrease of the dc term in the FT is highly desirable. Two different codification schemes are considered: binary pi radians phase modulation and hybrid ternary modulation. Any deviation in the values of the amplitude and phase shift generates the appearance of a strong dc term. Experimental results confirm that the calculated configurations provide a FT with no dc term, thus showing the effectiveness of the proposal.

Two different types of multiplexing are used to store 90 holograms at the same location in a polyvinyl alcoholacrylamide photopolymer material. In the first, the 90 holograms are stored using only peristrophic multiplexing, whereas in the second a combination of angular and peristrophic multiplexing is used. The results (diffraction efficiency and dynamic range, M#) obtained with these two multiplexing techniques are compared. With the first, the dynamic range was M# = 13 and with the second M# = 8. An exposure schedule method is used to calculate the exposure time necessary to store the holograms with a more uniform, higher diffraction efficiency.

In order to use photopolymers in the recording of holographic memories, high physical thickness is required. This generates many problems associated with the attenuation of light in the recording due to Beer's law. One of the more significant disadvantages is the fact that there are differences between the physical thickness of the material and the optical thickness of the holograms recorded. The optical thickness characterizes the angular selectivity of the holograms and determines the separation between two consecutive holograms in angular peristrophic multiplexing. In this work we propose a new method to record many holograms multiplexed with similar diffraction efficiency values taking into account the different effective optical thickness of each hologram.

The capability of polyvinyl alcohol-acrylamide photopolymer materials to obtain angularly multiplexed holographic gratings has been demonstrated [Appl. Phys. B 76, 851 (2003)]. A combination of two multiplexing methods--peristrophic and angular multiplexing--is used to record 60 holograms. An exposure schedule method is used to optimize the capability of the photopolymerizable holographic material and obtain holograms with a higher, more uniform diffraction efficiency. In addition, because of this exposure schedule method, the entire dynamic range (M#) of the material will be exploited, obtaining values of approximately M# approximately 9 in layers approximately 800 microm thick.

Large thickness is required in holographic recording materials to be used as holographic memories. Photopolymers have proved to be a good alternative to construct holographic memories. Nevertheless, modeling the behavior of thick layers poses some problems due to high absorption of the dye, as discussed in previous papers. In this study, the gratings stored in photopolymers based on PVA/AA are analyzed considering the attenuation of light in depth. This is done by fitting the theoretical results, predicted by a model that considers this effect, to the experimental results obtained using diffraction gratings recorded in PVA/AA based photopolymer. In order to determine the diffraction efficiency at the first Bragg angle, an algorithm based on the rigorous coupled wave theory is used. Also, the characteristics of the gratings obtained using different recording intensities are analyzed, and the effective optical thickness is seen to increase as the intensity is increased.

Several theoretical models have been proposed to predict the behavior of photopolymers as holographic recording materials. Basically these models have been applied to study thin layers (around 100 microm thick). The increasing importance of holographic memories recorded in photopolymers (thickness of > 500 microm) makes it necessary to extend the ideas proposed by these models to study thick photopolymer layers. We calculate the temporal evolution of the diffraction efficiencies for thick layers using a first-harmonic diffusion model, and the results obtained are compared with the corresponding values for thin layers. Furthermore, the values of the average diffusivity of the polymer chains after the grating is formed are also obtained. In general, we find that the monomer and polymer diffusivity increases when higher values of thickness are used.

The nonlocal polymerization-driven diffusion model (NPDD) has been shown to predict high spatial frequency cut-off in photopolymers and to accurately predict higher order grating components. We propose an extension to the NPDD model to account for the temporal response associated with polymer chain growth. An exponential response function is proposed to describe transient effects during the polymerization process. The extended model is then solved using a finite element technique and the nature of grating evolution examined in the case when illumination is stopped prior to the saturation of the grating recording process. Based on independently determined refractive index measurements we determine the temporal evolution of the refractive index modulation and the resulting diffraction efficiency using rigorous coupled wave theory. Material parameters are then extracted based on fits to experimental data for nonlinear and both ideal and non-ideal kinetic models.

We have corrected typing errors related to the characterization of the dynamic range of the acrylamide photopolymer described in an earlier study [Appl. Opt. 42, 7008 (2003)]. The M number is expressed as M/# instead of M# as appears in the text. The value calculated from the experimental results that are included in the article is M/# = 3.8 instead of 38 as appears in the text.

Poly(vinyl alcohol-acrylamide) photopolymers are materials of interest in the field of digital information storage (holographic memories). We analyzed the behavior of a 1-mm-thick photopolymer. Using a standard holographic setup, we recorded unslanted diffraction gratings. The material has high angular selectivity (0.4 degrees), good sensitivity (88 mJ/cm2), and small losses caused by absorption and scattering of light. It also has a high maximum diffraction efficiency (70%). A significant induction period was seen in the material. The authors hypothesize that, during most of this induction period, polymerization does in fact take place but is not reflected in the appearance of the diffracted light until a certain threshold value of exposure is reached.

Photopolymers are interesting materials for use in recording information in holography. We study the holographic behavior and stability of volume holograms recorded in poly(vinyl alcohol)--acrylamide photopolymers with and without a cross linker. Using a first-harmonic diffusion model, we analyze the residual monomer that remains when volume diffraction gratings are recorded in photopolymer materials. The importance of this residual monomer to the stability of the gratings is evaluated.

We demonstrate edge-enhanced imaging produced by volume phase gratings recorded on a polyvinyl alcohol/acrylamide photopolymer. Bragg diffraction, exhibited by volume gratings, modifies the impulse response of the imaging system, facilitating spatial filtering operations with no need for a physical Fourier plane. We demonstrate that Kogelnik's coupled-wave theory can be used to calculate the transfer function for the transmitted and the diffracted orders. The experimental and simulated results agree, and they demonstrate the feasibility of our proposal.

The nonlocal diffusion model proposed by Sheridan and coworkers has provided a useful interpretation of the nature of grating formation inside photopolymer materials. This model accounts for some important experimental facts, such as the cut-off of diffraction efficiency for high spatial frequencies. In this article we examine the predictions of the model in the case of a general dependence of the polymerisation rate with respect to the intensity pattern. The effects of this dependence on the different harmonic components of the polymerisation concentration will be investigated. The influence of the visibility on the different harmonic components will also be studied. These effects are compared to the effects of varying RD and sigmaD.

Some of the theoretical models in the literature describing the mechanism of hologram formation in photopolymer materials predict the existence of higher harmonics in the Fourier expansion of the recorded refractive index. Nevertheless, quantitative information is only obtained for the first harmonic of the refractive index using Kogelnik's Coupled Wave Theory. In this work we apply the Rigorous Coupled Wave Theory to demonstrate that when recording phase diffraction gratings in PVA/acrylamide photopolymer materials, a second order grating is also recorded in the hologram even when the material is exposed to a sinusoidal interference pattern. The influence of this second order grating on the efficiency of the first order for replay at the first on-Bragg angular replay condition is studied and the size of the 2nd harmonic examined.